Your browser doesn't support javascript.
loading
Circulating cytokines and small molecules follow distinct expression patterns in acute myeloid leukaemia.
Islam, Mirazul; Mohamed, Elsa Haniffah; Esa, Ezalia; Kamaluddin, Nor Rizan; Zain, Shamsul Mohd; Yusoff, Yuslina Mat; Assenov, Yassen; Mohamed, Zahurin; Zakaria, Zubaidah.
Afiliación
  • Islam M; Department of Medical Oncology, Dana-Farber Cancer Institute, 44 Binney Street, Boston, MA 02115, USA.
  • Mohamed EH; Cancer Program, The Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
  • Esa E; Pharmacogenomics Lab, Department of Pharmacology, Faculty of Medicine, University of Malaya, Kuala Lumpur 50603, Malaysia.
  • Kamaluddin NR; Pharmacogenomics Lab, Department of Pharmacology, Faculty of Medicine, University of Malaya, Kuala Lumpur 50603, Malaysia.
  • Zain SM; Haematology Unit, Cancer Research Centre, Institute for Medical Research, Jalan Pahang, Kuala Lumpur 50588, Malaysia.
  • Yusoff YM; Haematology Unit, Cancer Research Centre, Institute for Medical Research, Jalan Pahang, Kuala Lumpur 50588, Malaysia.
  • Assenov Y; Pharmacogenomics Lab, Department of Pharmacology, Faculty of Medicine, University of Malaya, Kuala Lumpur 50603, Malaysia.
  • Mohamed Z; Haematology Unit, Cancer Research Centre, Institute for Medical Research, Jalan Pahang, Kuala Lumpur 50588, Malaysia.
  • Zakaria Z; Computational Epigenomics Group, Division of Epigenomics and Cancer Risk Factor, German Cancer Research Center, Heidelberg 69120, Germany.
Br J Cancer ; 117(10): 1551-1556, 2017 Nov 07.
Article en En | MEDLINE | ID: mdl-28898234
ABSTRACT

BACKGROUND:

Although aberrant expression of cytokines and small molecules (analytes) is well documented in acute myeloid leukaemia (AML), their co-expression patterns are not yet identified. In addition, plasma baselines for some analytes that are biomarkers for other cancers have not been previously reported in AML.

METHODS:

We used multiplex array technology to simultaneously detect and quantify 32 plasma analyte (22 reported analytes and 10 novel analytes) levels in 38 patients.

RESULTS:

In our study, 16 analytes are found to be significantly deregulated (13 higher, 3 lower, Mann-Whitney U-test, P-value <0.005), where 5 of them have never been reported before in AML. We predicted a seven-analyte-containing multiplex panel for diagnosis of AML and, among them, MIF could be a possible therapeutic target. In addition, we observed that circulating analytes show five co-expression signatures.

CONCLUSIONS:

Circulating analyte expression in AML significantly differs from normal, and follow distinct expression patterns.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Leucemia Mieloide Aguda / Biomarcadores de Tumor / Citocinas Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Br J Cancer Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Leucemia Mieloide Aguda / Biomarcadores de Tumor / Citocinas Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Br J Cancer Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos